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FDA 510(k)

ACETATE CONCENTRATES FOR HEMODIALYSIS

K-Number: K905021 · 1991-03-15

Decision Date1991-03-15
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACETATE CONCENTRATES FOR HEMODIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1991-03-15 under 510(k) number K905021. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETATE CONCENTRATES FOR HEMODIALYSIS?

ACETATE CONCENTRATES FOR HEMODIALYSIS is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Medical Components, Inc.. The 510(k) number is K905021.

When did ACETATE CONCENTRATES FOR HEMODIALYSIS receive FDA 510(k) clearance?

ACETATE CONCENTRATES FOR HEMODIALYSIS received FDA 510(k) clearance on 1991-03-15, under 510(k) number K905021.

Who is the listed applicant for ACETATE CONCENTRATES FOR HEMODIALYSIS?

The FDA 510(k) record lists Medical Components, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACETATE CONCENTRATES FOR HEMODIALYSIS?

The FDA product code for ACETATE CONCENTRATES FOR HEMODIALYSIS is KPO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medical Components, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 61 devices →

Related Devices (Code: KPO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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